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Cosmetics and personal care

Which rules apply to eye make-up?

We track 6,776 rules for these in 20 of 21 markets, including California's Prop 65 list of 883 chemicals. Check your product free, no account needed.

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Cosmetics and personal care / Make-up / Eye make-up

Mascara, eyeliner, eye shadow and brow products for the eye area.

Rules

Rules by market

Open a market to read its rules for this category.

European Union2,230 rulesCoverage: Main sources, from 18 May 2026
Main sources, from 18 May 2026 · What is covered

European Union: main sources stored. Modelled: Reg. 1223/2009 Annexes II (prohibited); III (restricted); IV (colourants); V (preservatives); VI (UV filters) and Art. 19 labelling; Arts. 4 to 13: Responsible Person, safety assessment and safety report (CPSR), product information file (PIF), CPNP notification. Not stored: CLP classification and labelling of cosmetic mixtures; REACH Annex XVII entries beyond cosmetics (e.g. microplastics Reg. 2023/2055); national rules (e.g. French recycling labels, German language rules); claims criteria (Reg. 655/2013); packaging law (PPWR); Annex III-VI entries adopted after the stored consolidation.

Requirement
Applies when
Effective
Source
Conformity
Talc (Talc: Hydrated magnesium silicate; CAS 14807-96-6)

Must meet the conditions of Annex III entry 59: (a) Powdery products intended to be used for children under 3 years of age (b) Other products

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Intended for children under 3

Depends on: intended for children under 3

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

From the consolidated text: Talc · 14807-96-6 · 238-877-9 · (a) Powdery products intended to be used for children under 3 years of age (b) Other products

Label
Talc (Talc: Hydrated magnesium silicate; CAS 14807-96-6)

Label required

(a) Keep powder away from children's nose and mouth

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Intended for children under 3

Depends on: intended for children under 3

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

“(a) Keep powder away from children's nose and mouth”
Annex III entry 59 (wording) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
Label
5-Bromo-5-nitro-1,3-dioxane (CAS 30007-47-7)

Label required

Avoid formation of nitrosamines

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Rinse-off product

Depends on: rinse off

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

“Avoid formation of nitrosamines”
Annex V entry 20 (wording) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
Label
Thimerosal (Thiomersal; CAS 54-64-8)

Label required

Contains Thiomersal

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Applied to: Eye area

Depends on: body area

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

“Contains Thiomersal”
Annex V entry 16 (wording) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
Label
Phenyl Mercuric Acetate (Phenylmercuric salts (including borate); CAS 62-38-4)

Label required

Contains Phenylmercuric compounds

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Applied to: Eye area

Depends on: body area

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

“Contains Phenylmercuric compounds”
Annex V entry 17 (wording) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
Label
Butylparaben propylparaben sodium propylparaben sodium butylparaben potassium butylparaben potassium propylparaben (CAS 94-26-8)

Label required

For leave-on products designed for children under three years of age: ‘Do not use on the nappy area’

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Leave-on product
  • Intended for children under 3

Depends on: rinse off, intended for children under 3

In force, start date unknown

No date for this row is stated in the published text (consolidation marker M8; the amending act's application date is not printed). In force no later than 2026-05-18 (the date of the version ClaraDB holds); earlier commencement is not stated in the published text.

“For leave-on products designed for children under three years of age: ‘Do not use on the nappy area’”
Annex V entry 12a (wording) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
Conformity

Corrective measures where a product placed on the market is not in conformity

Must meet the conditions of Art. 5(2): immediately take the corrective measures necessary to bring the product into conformity, withdraw it or recall it

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Responsible persons who consider or have reason to believe that a cosmetic product which they have placed on the market is not in conformity with this Regulation shall immediately take the corrective measures necessary to bring that product into conformity, withdraw it or recall it, as appropriate.”
Art. 5(2) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity

Manufacture must follow good manufacturing practice

Must meet the conditions of Art. 8(1): manufacture complies with good manufacturing practice (presumed where manufacture follows the harmonised standards published in the Official Journal, Art. 8(2))

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products manufactured on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“The manufacture of cosmetic products shall comply with good manufacturing practice with a view to ensuring the objectives of Article 1.”
Art. 8(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity

Art. 10(2)

Must meet the conditions of Art. 10(2): the cosmetic product safety assessment (Annex I Part B) is carried out by a person with a diploma or formal qualification in pharmacy, toxicology, medicine or a similar discipline

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products manufactured on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“shall be carried out by a person in possession of a diploma or other evidence of formal qualifications”
Art. 10(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Art. 13(2)

Notification to Commission (CPNP)

Original labelling and, where reasonably legible, a photograph of the corresponding packaging

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“the responsible person shall notify to the Commission the original labelling, and, where reasonably legible, a photograph of the corresponding packaging”
Art. 13(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Product notification before placing on the market (EU CPNP / GB SCPN)

Notification to European Commission (CPNP)

Category and name of the product; name and address of the responsible person where the product information file is kept; country of origin if imported; Member State of placing on the market; contact details of a natural person; presence of nanomaterials and their identification and reasonably foreseeable exposure conditions; name and CAS or EC number of CMR 1A/1B substances; frame formulation; original labelling and, where legible, a photograph of the packaging (Art. 13(2))

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Prior to placing the cosmetic product on the market the responsible person shall submit, by electronic means, the following information to the Commission:”
Art. 13(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Notification of authorities where the product presents a risk to human health

Notification to Competent national authorities of the Member States in which the product was made available and of the Member State where the product information file is readily accessible

Details of the non-compliance and of the corrective measures taken

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Furthermore, where the cosmetic product presents a risk to human health, responsible persons shall immediately inform the competent national authorities of the Member States”
Art. 5(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity

Art. 6(1)

Must meet the conditions of Art. 6(1): act with due care in relation to applicable requirements when making a cosmetic product available

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“distributors shall act with due care in relation to applicable requirements”
Art. 6(1) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity

Art. 6(3)

Must meet the conditions of Art. 6(3): do not make a non-conforming product available until it is brought into conformity; ensure corrective measures, withdrawal or recall for products already made available

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“they shall not make the product available on the market until it has been brought into conformity with the applicable requirements”
Art. 6(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity

Art. 6(4)

Must meet the conditions of Art. 6(4): storage or transport conditions under the distributor's responsibility do not jeopardise compliance

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“storage or transport conditions do not jeopardise its compliance with the requirements set out in this Regulation”
Art. 6(4) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Distributor informs RP and authorities of risk

Notification to Responsible person and competent authorities

Details of non-compliance and corrective measures taken

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Furthermore, where the cosmetic product presents a risk to human health, distributors shall immediately inform the responsible person and the competent national authorities of the Member States”
Art. 6(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Distributor that translates labelling notifies the Commission

Notification to European Commission (CPNP)

Category, names in both Member States, Member State of availability, distributor name and address, responsible person

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 13(3): 'As from 11 July 2013' (stated in the provision); Art. 40(2) is consistent.

“a distributor who makes available in a Member State a cosmetic product already placed on the market in another Member State and translates, on his own initiative, any element of the labelling of that product in order to comply with national law, shall submit, by electronic means, the following information to the Commission”
Art. 13(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Test

Distributors verify labelling, language and durability before making available

Test required

Distributor verification before making a product available: labelling information (Art. 19(1)(a), (e), (g), 19(3)-(4)), language requirements and date of minimum durability

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Before making a cosmetic product available on the market distributors shall verify that:”
Art. 6(2) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Label

Mandatory label element: nominal content

Label required

Nominal content at the time of packaging by weight or volume

Exemptions (1)

Free samples and single-application packs; pre-packages normally sold as a number of items where the number appears on the packaging or is easy to see from outside

“free samples and single-application packs”
Art. 19(1)(b) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Net content at least 5 mL

Depends on: net content ml

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“the nominal content at the time of packaging, given by weight or by volume, except in the case of packaging containing less than five grams or five millilitres, free samples and single-application packs”
Art. 19(1)(b) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Notification of cosmetic products containing nanomaterials six months before placing on the market

Notification to European Commission

Nanomaterial identification (IUPAC name and descriptors), specification (particle size, physical and chemical properties), estimated annual quantity, toxicological profile, safety data for the product category, reasonably foreseeable exposure conditions; six months before placing on the market

Exemptions (2)

Not applicable to cosmetic products containing nanomaterials in conformity with Annex III

“shall not apply to cosmetic products containing nanomaterials that are in conformity with the requirements set out in Annex III”
Art. 16(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

Art. 16 does not apply to nanomaterials used as colorants, UV-filters or preservatives regulated under Article 14, unless expressly specified

“do not apply to nanomaterials used as colorants, UV-filters or preservatives regulated under Article 14”
Art. 16(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Contains a nanomaterial
  • Your role: Manufacturer or Importer

Depends on: contains nanomaterial, economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the first subparagraph of Art. 16(3) applies from 11 July 2013 with the Regulation; only the second subparagraph (products already on the market, notification between 11 January 2013 and 11 July 2013) applies from 11 January 2013 and is a transitional duty not listed as a separate rule.

“cosmetic products containing nanomaterials shall be notified to the Commission by the responsible person by electronic means six months prior to being placed on the market”
Art. 16(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity

A no-animal-test claim is allowed only where no animal tests were carried out or commissioned

Must meet the conditions of Art. 20(3): a no-animal-testing claim only if neither the manufacturer nor its suppliers carried out or commissioned animal tests on the finished product, prototype or ingredients, or used ingredients tested on animals by others for developing new cosmetic products

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Claim: not tested on animals

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“to the fact that no animal tests have been carried out only if the manufacturer and his suppliers have not carried out or commissioned any animal tests”
Art. 20(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Update of notified information when it changes

Notification to European Commission (CPNP)

Update, without delay, of any changed information notified under Art. 13(1), (3) or (4)

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer or Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Where any of the information set out in paragraphs 1, 3 and 4 changes, the responsible person or the distributor shall provide an update without delay.”
Art. 13(7) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Notify serious undesirable effects

Notification to Competent authority of the Member State where the serious undesirable effect occurred

All serious undesirable effects known or reasonably expected to be known, the name of the product enabling identification, and any corrective measures taken

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer or Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“In the event of serious undesirable effects, the responsible person and distributors shall without delay notify the following to the competent authority of the Member State where the serious undesirable effect occurred:”
Art. 23(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Disclosure

PIF accessible to authority at address on label, in understandable language

Disclosure to authority

Make the product information file readily accessible at the address on the label, in a language easily understood by the authority

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“The responsible person shall make the product information file readily accessible in electronic or other format at his address indicated on the label to the competent authority of the Member State in which the file is kept.”
Art. 11(3) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Disclosure

Public access to composition and undesirable effect data

Disclosure to consumer

Qualitative and quantitative composition (quantitative information limited to hazardous substances under CLP Art. 3), for perfume compositions the name, code number and supplier, and existing data on undesirable and serious undesirable effects, made easily accessible to the public

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“the responsible person shall ensure that the qualitative and quantitative composition of the cosmetic product and, in the case of perfume and aromatic compositions, the name and code number of the composition and the identity of the supplier, as well as existing data on undesirable effects and serious undesirable effects”
Art. 21 (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity
    Talc (Talc: Hydrated magnesium silicate; CAS 14807-96-6)

    Must meet the conditions of Annex III entry 59: (a) Powdery products intended to be used for children under 3 years of age (b) Other products

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Intended for children under 3

    Depends on: intended for children under 3

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

    Source

    From the consolidated text: Talc · 14807-96-6 · 238-877-9 · (a) Powdery products intended to be used for children under 3 years of age (b) Other products

  • Label
    Talc (Talc: Hydrated magnesium silicate; CAS 14807-96-6)

    Label required

    (a) Keep powder away from children's nose and mouth

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Intended for children under 3

    Depends on: intended for children under 3

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

    Source
    “(a) Keep powder away from children's nose and mouth”
    Annex III entry 59 (wording) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
  • Label
    5-Bromo-5-nitro-1,3-dioxane (CAS 30007-47-7)

    Label required

    Avoid formation of nitrosamines

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Rinse-off product

    Depends on: rinse off

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

    Source
    “Avoid formation of nitrosamines”
    Annex V entry 20 (wording) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
  • Label
    Thimerosal (Thiomersal; CAS 54-64-8)

    Label required

    Contains Thiomersal

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Applied to: Eye area

    Depends on: body area

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

    Source
    “Contains Thiomersal”
    Annex V entry 16 (wording) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
  • Label
    Phenyl Mercuric Acetate (Phenylmercuric salts (including borate); CAS 62-38-4)

    Label required

    Contains Phenylmercuric compounds

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Applied to: Eye area

    Depends on: body area

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

    Source
    “Contains Phenylmercuric compounds”
    Annex V entry 17 (wording) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
  • Label
    Butylparaben propylparaben sodium propylparaben sodium butylparaben potassium butylparaben potassium propylparaben (CAS 94-26-8)

    Label required

    For leave-on products designed for children under three years of age: ‘Do not use on the nappy area’

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Leave-on product
    • Intended for children under 3

    Depends on: rinse off, intended for children under 3

    Effective

    In force, start date unknown

    No date for this row is stated in the published text (consolidation marker M8; the amending act's application date is not printed). In force no later than 2026-05-18 (the date of the version ClaraDB holds); earlier commencement is not stated in the published text.

    Source
    “For leave-on products designed for children under three years of age: ‘Do not use on the nappy area’”
    Annex V entry 12a (wording) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
  • Conformity

    Corrective measures where a product placed on the market is not in conformity

    Must meet the conditions of Art. 5(2): immediately take the corrective measures necessary to bring the product into conformity, withdraw it or recall it

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Responsible persons who consider or have reason to believe that a cosmetic product which they have placed on the market is not in conformity with this Regulation shall immediately take the corrective measures necessary to bring that product into conformity, withdraw it or recall it, as appropriate.”
    Art. 5(2) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    Manufacture must follow good manufacturing practice

    Must meet the conditions of Art. 8(1): manufacture complies with good manufacturing practice (presumed where manufacture follows the harmonised standards published in the Official Journal, Art. 8(2))

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products manufactured on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “The manufacture of cosmetic products shall comply with good manufacturing practice with a view to ensuring the objectives of Article 1.”
    Art. 8(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    Art. 10(2)

    Must meet the conditions of Art. 10(2): the cosmetic product safety assessment (Annex I Part B) is carried out by a person with a diploma or formal qualification in pharmacy, toxicology, medicine or a similar discipline

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products manufactured on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “shall be carried out by a person in possession of a diploma or other evidence of formal qualifications”
    Art. 10(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Art. 13(2)

    Notification to Commission (CPNP)

    Original labelling and, where reasonably legible, a photograph of the corresponding packaging

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “the responsible person shall notify to the Commission the original labelling, and, where reasonably legible, a photograph of the corresponding packaging”
    Art. 13(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Product notification before placing on the market (EU CPNP / GB SCPN)

    Notification to European Commission (CPNP)

    Category and name of the product; name and address of the responsible person where the product information file is kept; country of origin if imported; Member State of placing on the market; contact details of a natural person; presence of nanomaterials and their identification and reasonably foreseeable exposure conditions; name and CAS or EC number of CMR 1A/1B substances; frame formulation; original labelling and, where legible, a photograph of the packaging (Art. 13(2))

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Prior to placing the cosmetic product on the market the responsible person shall submit, by electronic means, the following information to the Commission:”
    Art. 13(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Notification of authorities where the product presents a risk to human health

    Notification to Competent national authorities of the Member States in which the product was made available and of the Member State where the product information file is readily accessible

    Details of the non-compliance and of the corrective measures taken

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Furthermore, where the cosmetic product presents a risk to human health, responsible persons shall immediately inform the competent national authorities of the Member States”
    Art. 5(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    Art. 6(1)

    Must meet the conditions of Art. 6(1): act with due care in relation to applicable requirements when making a cosmetic product available

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “distributors shall act with due care in relation to applicable requirements”
    Art. 6(1) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    Art. 6(3)

    Must meet the conditions of Art. 6(3): do not make a non-conforming product available until it is brought into conformity; ensure corrective measures, withdrawal or recall for products already made available

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “they shall not make the product available on the market until it has been brought into conformity with the applicable requirements”
    Art. 6(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    Art. 6(4)

    Must meet the conditions of Art. 6(4): storage or transport conditions under the distributor's responsibility do not jeopardise compliance

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “storage or transport conditions do not jeopardise its compliance with the requirements set out in this Regulation”
    Art. 6(4) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Distributor informs RP and authorities of risk

    Notification to Responsible person and competent authorities

    Details of non-compliance and corrective measures taken

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Furthermore, where the cosmetic product presents a risk to human health, distributors shall immediately inform the responsible person and the competent national authorities of the Member States”
    Art. 6(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Distributor that translates labelling notifies the Commission

    Notification to European Commission (CPNP)

    Category, names in both Member States, Member State of availability, distributor name and address, responsible person

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 13(3): 'As from 11 July 2013' (stated in the provision); Art. 40(2) is consistent.

    Source
    “a distributor who makes available in a Member State a cosmetic product already placed on the market in another Member State and translates, on his own initiative, any element of the labelling of that product in order to comply with national law, shall submit, by electronic means, the following information to the Commission”
    Art. 13(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Test

    Distributors verify labelling, language and durability before making available

    Test required

    Distributor verification before making a product available: labelling information (Art. 19(1)(a), (e), (g), 19(3)-(4)), language requirements and date of minimum durability

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Before making a cosmetic product available on the market distributors shall verify that:”
    Art. 6(2) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Label

    Mandatory label element: nominal content

    Label required

    Nominal content at the time of packaging by weight or volume

    Exemptions (1)

    Free samples and single-application packs; pre-packages normally sold as a number of items where the number appears on the packaging or is easy to see from outside

    “free samples and single-application packs”
    Art. 19(1)(b) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Net content at least 5 mL

    Depends on: net content ml

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “the nominal content at the time of packaging, given by weight or by volume, except in the case of packaging containing less than five grams or five millilitres, free samples and single-application packs”
    Art. 19(1)(b) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Notification of cosmetic products containing nanomaterials six months before placing on the market

    Notification to European Commission

    Nanomaterial identification (IUPAC name and descriptors), specification (particle size, physical and chemical properties), estimated annual quantity, toxicological profile, safety data for the product category, reasonably foreseeable exposure conditions; six months before placing on the market

    Exemptions (2)

    Not applicable to cosmetic products containing nanomaterials in conformity with Annex III

    “shall not apply to cosmetic products containing nanomaterials that are in conformity with the requirements set out in Annex III”
    Art. 16(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

    Art. 16 does not apply to nanomaterials used as colorants, UV-filters or preservatives regulated under Article 14, unless expressly specified

    “do not apply to nanomaterials used as colorants, UV-filters or preservatives regulated under Article 14”
    Art. 16(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Contains a nanomaterial
    • Your role: Manufacturer or Importer

    Depends on: contains nanomaterial, economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the first subparagraph of Art. 16(3) applies from 11 July 2013 with the Regulation; only the second subparagraph (products already on the market, notification between 11 January 2013 and 11 July 2013) applies from 11 January 2013 and is a transitional duty not listed as a separate rule.

    Source
    “cosmetic products containing nanomaterials shall be notified to the Commission by the responsible person by electronic means six months prior to being placed on the market”
    Art. 16(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    A no-animal-test claim is allowed only where no animal tests were carried out or commissioned

    Must meet the conditions of Art. 20(3): a no-animal-testing claim only if neither the manufacturer nor its suppliers carried out or commissioned animal tests on the finished product, prototype or ingredients, or used ingredients tested on animals by others for developing new cosmetic products

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Claim: not tested on animals
    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “to the fact that no animal tests have been carried out only if the manufacturer and his suppliers have not carried out or commissioned any animal tests”
    Art. 20(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Update of notified information when it changes

    Notification to European Commission (CPNP)

    Update, without delay, of any changed information notified under Art. 13(1), (3) or (4)

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer or Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Where any of the information set out in paragraphs 1, 3 and 4 changes, the responsible person or the distributor shall provide an update without delay.”
    Art. 13(7) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Notify serious undesirable effects

    Notification to Competent authority of the Member State where the serious undesirable effect occurred

    All serious undesirable effects known or reasonably expected to be known, the name of the product enabling identification, and any corrective measures taken

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer or Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “In the event of serious undesirable effects, the responsible person and distributors shall without delay notify the following to the competent authority of the Member State where the serious undesirable effect occurred:”
    Art. 23(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Disclosure

    PIF accessible to authority at address on label, in understandable language

    Disclosure to authority

    Make the product information file readily accessible at the address on the label, in a language easily understood by the authority

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “The responsible person shall make the product information file readily accessible in electronic or other format at his address indicated on the label to the competent authority of the Member State in which the file is kept.”
    Art. 11(3) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Disclosure

    Public access to composition and undesirable effect data

    Disclosure to consumer

    Qualitative and quantitative composition (quantitative information limited to hazardous substances under CLP Art. 3), for perfume compositions the name, code number and supplier, and existing data on undesirable and serious undesirable effects, made easily accessible to the public

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “the responsible person shall ensure that the qualitative and quantitative composition of the cosmetic product and, in the case of perfume and aromatic compositions, the name and code number of the composition and the identity of the supplier, as well as existing data on undesirable effects and serious undesirable effects”
    Art. 21 (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

Gaps

Markets without rules for this category

We have no rules for this category in these markets. That doesn't mean none apply, so a check here says Not covered, never clear.

ClaraDB gives a verdict only for PFAS state laws for cookware and bakeware, California Proposition 65 consumer-product warning check for BPA, BPS, formaldehyde, styrene, antimony trioxide, vinyl acetate, lead and cadmium, California Proposition 65 warning check for candles and ceramicware (lead, cadmium, formaldehyde, acetaldehyde, benzene, naphthalene, carbon monoxide, benzo[a]pyrene), US packaging EPR producer size thresholds (California, Colorado, Maryland, Minnesota, Oregon, Washington) for a brand-owning manufacturer, US lead in children's products and furniture (lead paint and total lead content), US lead in toys and child care articles (lead paint and total lead content), US lead in children's products (other) and bags (lead paint and total lead content), US phthalates in children's toys and child care articles (DEHP, DBP, BBP, DINP, DIBP, DPENP, DHEXP, DCHP) and US children's product certificate and tracking label for children's tableware (AI-checked, quotes verified word for word). Every other answer shows the laws and quotes found without saying whether they apply. Not checked: Consumer electronics (FCC equipment authorization, 47 CFR Parts 2 and 15, energy rules). What ClaraDB has checked

Show 1 market
Market
Coverage
Main sources; no modeled rule is scoped to this category. Not covered: other rules that may apply.
  • Coverage
    Main sources; no modeled rule is scoped to this category. Not covered: other rules that may apply.

Facts

What we need to know about your product

Some rules depend on details of your product. Until you tell us, a check says Needs answers and asks for what's missing.

Show 36 facts
Depends on
Markets
Rules
Whether the listed substance or group is present
EU, GB, JP, KR, US, US-CA, US-CO, US-CT, US-IL, US-MD, US-ME, US-MN, US-NJ, US-RI, US-VT, US-WA
7,475
Number of employees at the seller
US-CA
972
Body area
EU, GB, JP, KR, US
231
Rinse off
EU, GB, JP, KR, US-CA
221
Economic operator role
EU, GB, KR, US
90
Contains battery
EU, GB, US
39
Sprayable
EU, GB, KR
34
Intended for children under 3
EU, GB, KR
24
Battery category
EU, GB
22
Otc drug claim
US, US-MN
19
Quasi drug or functional claim
JP, KR
13
Net content ml
EU, GB, KR
10
Battery chemistry
US
9
Aerosol dispenser
JP, KR, US
8
Professional use
EU, GB, US
7
Customised cosmetic
KR
7
Rechargeable
US
6
Animal testing conducted
EU, GB, KR
5
Annual gross revenue usd
US-CO, US-MD, US-MN, US-OR, US-WA
5
Contains nanomaterial
EU, GB
2
Intended for children under 12
KR
2
Single use
KR
2
Button or coin cell
US
2
Distance sale to other member state
EU
1
Imported
KR
1
Cattle derived material
US
1
Uses sunscreen term
US
1
Safety substantiated
US
1
Battery removable
US
1
Ca gross sales usd
US-CA
1
Packaging tons co
US-CO
1
Packaging tons md
US-MD
1
Packaging tons mn
US-MN
1
Packaging tonnes or
US-OR
1
Fluorine treated container
US-VT
1
Packaging tons wa
US-WA
1
  • Whether the listed substance or group is present
    Markets
    EU, GB, JP, KR, US, US-CA, US-CO, US-CT, US-IL, US-MD, US-ME, US-MN, US-NJ, US-RI, US-VT, US-WA
    Rules
    7,475
  • Number of employees at the seller
    Markets
    US-CA
    Rules
    972
  • Body area
    Markets
    EU, GB, JP, KR, US
    Rules
    231
  • Rinse off
    Markets
    EU, GB, JP, KR, US-CA
    Rules
    221
  • Economic operator role
    Markets
    EU, GB, KR, US
    Rules
    90
  • Contains battery
    Markets
    EU, GB, US
    Rules
    39
  • Sprayable
    Markets
    EU, GB, KR
    Rules
    34
  • Intended for children under 3
    Markets
    EU, GB, KR
    Rules
    24
  • Battery category
    Markets
    EU, GB
    Rules
    22
  • Otc drug claim
    Markets
    US, US-MN
    Rules
    19
  • Quasi drug or functional claim
    Markets
    JP, KR
    Rules
    13
  • Net content ml
    Markets
    EU, GB, KR
    Rules
    10
  • Battery chemistry
    Markets
    US
    Rules
    9
  • Aerosol dispenser
    Markets
    JP, KR, US
    Rules
    8
  • Professional use
    Markets
    EU, GB, US
    Rules
    7
  • Customised cosmetic
    Markets
    KR
    Rules
    7
  • Rechargeable
    Markets
    US
    Rules
    6
  • Animal testing conducted
    Markets
    EU, GB, KR
    Rules
    5
  • Annual gross revenue usd
    Markets
    US-CO, US-MD, US-MN, US-OR, US-WA
    Rules
    5
  • Contains nanomaterial
    Markets
    EU, GB
    Rules
    2
  • Intended for children under 12
    Markets
    KR
    Rules
    2
  • Single use
    Markets
    KR
    Rules
    2
  • Button or coin cell
    Markets
    US
    Rules
    2
  • Distance sale to other member state
    Markets
    EU
    Rules
    1
  • Imported
    Markets
    KR
    Rules
    1
  • Cattle derived material
    Markets
    US
    Rules
    1
  • Uses sunscreen term
    Markets
    US
    Rules
    1
  • Safety substantiated
    Markets
    US
    Rules
    1
  • Battery removable
    Markets
    US
    Rules
    1
  • Ca gross sales usd
    Markets
    US-CA
    Rules
    1
  • Packaging tons co
    Markets
    US-CO
    Rules
    1
  • Packaging tons md
    Markets
    US-MD
    Rules
    1
  • Packaging tons mn
    Markets
    US-MN
    Rules
    1
  • Packaging tonnes or
    Markets
    US-OR
    Rules
    1
  • Fluorine treated container
    Markets
    US-VT
    Rules
    1
  • Packaging tons wa
    Markets
    US-WA
    Rules
    1

Changes

Upcoming changes

Rules for this category that start in the next 24 months, or are proposed or on hold.

Show 41 upcoming changes
Requirement
Applies when
Effective
Source
WarningUS-CA
N-Methyl-N-Formylhydrazine (CAS 758-17-8)

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to N-Methyl-N-Formylhydrazine, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 8 Dec 2026

Applies to products sold on or after 8 Dec 2026

Listed 2025-12-08 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
N-Methyl-N-Formylhydrazine
Type of toxicity
cancer
Listed by
the State's Qualified Experts (SQE)
CAS No.
758-17-8
Date listed
8 Dec 2025

Prop 65 list row: N-Methyl-N-Formylhydrazine · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Bisphenol S (BPS) (CAS 80-09-1)

Warning required when exposure exceeds the threshold (no MADL listed for this row)

This product can expose you to Bisphenol S (BPS), which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required for a reproductive toxicant where the exposure will produce no observable effect at 1,000 times the level in question (at or below the MADL).

“a warning is not required if the business causing the exposure can demonstrate that the exposure will produce no observable effect, even at 1,000 times the level in question.”
Appendix A (summary), Exposures that will produce no observable reproductive effect (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 8 Dec 2026

Applies to products sold on or after 8 Dec 2026

Listed 2025-12-08 (developmental). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Bisphenol S (BPS)
Type of toxicity
developmental toxicity
Listed by
the State's Qualified Experts (SQE)
CAS No.
80-09-1
Date listed
8 Dec 2025

Prop 65 list row: Bisphenol S (BPS) · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Tacrolimus (CAS 104987-11-3)

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to Tacrolimus, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 17 Jul 2027

Applies to products sold on or after 17 Jul 2027

Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Tacrolimus
Type of toxicity
cancer
Listed by
the Labor Code (LC)
CAS No.
104987-11-3
Date listed
17 Jul 2026

Prop 65 list row: Tacrolimus · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Hydrochlorothiazide

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to Hydrochlorothiazide, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 17 Jul 2027

Applies to products sold on or after 17 Jul 2027

Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Hydrochlorothiazide
Type of toxicity
cancer
Listed by
the Labor Code (LC)
CAS No.
58-93-5; 125727-50-6; 8049-49-8
Date listed
17 Jul 2026

Prop 65 list row: Hydrochlorothiazide · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Voriconazole

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to Voriconazole, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 17 Jul 2027

Applies to products sold on or after 17 Jul 2027

Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Voriconazole
Type of toxicity
cancer
Listed by
the Labor Code (LC)
CAS No.
137234-62-9; 188416-29-7; 173967-54-9
Date listed
17 Jul 2026

Prop 65 list row: Voriconazole · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Welding Fumes

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to Welding Fumes, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 17 Jul 2027

Applies to products sold on or after 17 Jul 2027

Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Welding Fumes
Type of toxicity
cancer
Listed by
the Labor Code (LC)
CAS No.
none given
Date listed
17 Jul 2026

Prop 65 list row: Welding Fumes · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
BanEU
Triphenyl Phosphate (CAS 115-86-6)

Banned

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

Every product in the category

Takes effect 1 Jan 2027

Applies to products placed on the market on or after 1 Jan 2027

Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

From the consolidated text: Triphenyl Phosphate (13) · 115-86-6 · 204-112-2

LimitEU
Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)

Limit 0.7 % (content basis)

In the finished (ready for use) cosmetic product. Maximum concentration cell: (f) 0,7 %. Field of application: (f) Body lotion.

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Applied to: Body

Depends on: body area

Takes effect 1 Jan 2027

Applies to products placed on the market on or after 1 Jan 2027

Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

From the consolidated text: (f) Body lotion · (f) 0,7 %

Limit x 11EU

11 rules from Regulation (EC) No 1223/2009 on cosmetic products, Annexes II-VI (consolidated)

Limit 0.2 % (content basis)

Show targets (11 of 11)

Every product in the category

1 Jan 2027

Each rule has its own date; open a target.

Example: Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)

From the consolidated text: (g) Face make-up and make-up remover products · (g) 0,2 %

LimitEU
Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)

Limit 0.004 % (content basis)

In the finished (ready for use) cosmetic product. Maximum concentration cell: (h) 0,004 %. Field of application: (h) Oral products.

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Applied to: Mouth or Teeth and gums

Depends on: body area

Takes effect 1 Jan 2027

Applies to products placed on the market on or after 1 Jan 2027

Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

From the consolidated text: (h) Oral products · (h) 0,004 %

  • WarningUS-CA
    N-Methyl-N-Formylhydrazine (CAS 758-17-8)

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to N-Methyl-N-Formylhydrazine, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 8 Dec 2026

    Applies to products sold on or after 8 Dec 2026

    Listed 2025-12-08 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    N-Methyl-N-Formylhydrazine
    Type of toxicity
    cancer
    Listed by
    the State's Qualified Experts (SQE)
    CAS No.
    758-17-8
    Date listed
    8 Dec 2025

    Prop 65 list row: N-Methyl-N-Formylhydrazine · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Bisphenol S (BPS) (CAS 80-09-1)

    Warning required when exposure exceeds the threshold (no MADL listed for this row)

    This product can expose you to Bisphenol S (BPS), which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required for a reproductive toxicant where the exposure will produce no observable effect at 1,000 times the level in question (at or below the MADL).

    “a warning is not required if the business causing the exposure can demonstrate that the exposure will produce no observable effect, even at 1,000 times the level in question.”
    Appendix A (summary), Exposures that will produce no observable reproductive effect (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 8 Dec 2026

    Applies to products sold on or after 8 Dec 2026

    Listed 2025-12-08 (developmental). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Bisphenol S (BPS)
    Type of toxicity
    developmental toxicity
    Listed by
    the State's Qualified Experts (SQE)
    CAS No.
    80-09-1
    Date listed
    8 Dec 2025

    Prop 65 list row: Bisphenol S (BPS) · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Tacrolimus (CAS 104987-11-3)

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to Tacrolimus, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 17 Jul 2027

    Applies to products sold on or after 17 Jul 2027

    Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Tacrolimus
    Type of toxicity
    cancer
    Listed by
    the Labor Code (LC)
    CAS No.
    104987-11-3
    Date listed
    17 Jul 2026

    Prop 65 list row: Tacrolimus · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Hydrochlorothiazide

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to Hydrochlorothiazide, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 17 Jul 2027

    Applies to products sold on or after 17 Jul 2027

    Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Hydrochlorothiazide
    Type of toxicity
    cancer
    Listed by
    the Labor Code (LC)
    CAS No.
    58-93-5; 125727-50-6; 8049-49-8
    Date listed
    17 Jul 2026

    Prop 65 list row: Hydrochlorothiazide · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Voriconazole

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to Voriconazole, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 17 Jul 2027

    Applies to products sold on or after 17 Jul 2027

    Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Voriconazole
    Type of toxicity
    cancer
    Listed by
    the Labor Code (LC)
    CAS No.
    137234-62-9; 188416-29-7; 173967-54-9
    Date listed
    17 Jul 2026

    Prop 65 list row: Voriconazole · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Welding Fumes

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to Welding Fumes, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 17 Jul 2027

    Applies to products sold on or after 17 Jul 2027

    Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Welding Fumes
    Type of toxicity
    cancer
    Listed by
    the Labor Code (LC)
    CAS No.
    none given
    Date listed
    17 Jul 2026

    Prop 65 list row: Welding Fumes · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • BanEU
    Triphenyl Phosphate (CAS 115-86-6)

    Banned

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when

    Every product in the category

    Effective

    Takes effect 1 Jan 2027

    Applies to products placed on the market on or after 1 Jan 2027

    Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

    Source

    From the consolidated text: Triphenyl Phosphate (13) · 115-86-6 · 204-112-2

  • LimitEU
    Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)

    Limit 0.7 % (content basis)

    In the finished (ready for use) cosmetic product. Maximum concentration cell: (f) 0,7 %. Field of application: (f) Body lotion.

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Applied to: Body

    Depends on: body area

    Effective

    Takes effect 1 Jan 2027

    Applies to products placed on the market on or after 1 Jan 2027

    Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

    Source

    From the consolidated text: (f) Body lotion · (f) 0,7 %

  • Limit x 11EU

    11 rules from Regulation (EC) No 1223/2009 on cosmetic products, Annexes II-VI (consolidated)

    Limit 0.2 % (content basis)

    Show targets (11 of 11)
    Applies when

    Every product in the category

    Effective

    1 Jan 2027

    Each rule has its own date; open a target.

    Source

    Example: Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)

    From the consolidated text: (g) Face make-up and make-up remover products · (g) 0,2 %

  • LimitEU
    Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)

    Limit 0.004 % (content basis)

    In the finished (ready for use) cosmetic product. Maximum concentration cell: (h) 0,004 %. Field of application: (h) Oral products.

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Applied to: Mouth or Teeth and gums

    Depends on: body area

    Effective

    Takes effect 1 Jan 2027

    Applies to products placed on the market on or after 1 Jan 2027

    Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

    Source

    From the consolidated text: (h) Oral products · (h) 0,004 %

All dated changes

Records

Recalls and alerts

Recalls, safety alerts and Prop 65 notices that name Eye make-up, with a link to the original. A Prop 65 notice is a claim by the sender, not a ruling.

235 records dated 3 Jan 2023 to 18 Sep 2026. Most recent shown.

Show the 8 most recent records

See also

Related categories

  • Make-up

    Colour cosmetics for face, eyes, lips and lashes.

  • Lip products

    Lipstick, gloss, balm and liner (ingested in small amounts; Annex IV colourants for lips).

  • Eyelash and eyebrow dyes and enhancers

    Lash and brow tints and growth serums; hair dye substances may not be used on eyelashes in the EU.

  • Face make-up

    Foundation, powder, blush, concealer and bronzer.

Alerts

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